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氮同位素为研究人类结直肠癌细胞中的氨基酸代谢提供了线索。

Nitrogen isotopes provide clues to amino acid metabolism in human colorectal cancer cells.

机构信息

Department of Geosciences, Western Michigan University, Kalamazoo, MI, 49008, USA.

Laboratory of Virology, Department of Biological Sciences, Western Michigan University, Kalamazoo, MI, 49008-5410, USA.

出版信息

Sci Rep. 2017 May 31;7(1):2562. doi: 10.1038/s41598-017-02793-y.

Abstract

Glutamic acid and alanine make up more than 60 per cent of the total amino acids in the human body. Glutamine is a significant source of energy for cells and also a prime donor of nitrogen in the biosynthesis of many amino acids. Several studies have advocated the role of glutamic acid in cancer therapy. Identification of metabolic signatures in cancer cells will be crucial for advancement of cancer therapies based on the cell's metabolic state. Stable nitrogen isotope ratios (N/N, δN) are of particular advantage to understand the metabolic state of cancer cells, since most biochemical reactions involve transfer of nitrogen. In our study, we used the natural abundances of nitrogen isotopes (δN values) of individual amino acids from human colorectal cancer cell lines to investigate isotope discrimination among amino acids. Significant effects were noticed in the case of glutamic acid, alanine, aspartic acid and proline between cancer and healthy cells. The data suggest that glutamic acid is a nitrogen acceptor while alanine, aspartic acid and proline are nitrogen donors in cancerous cells. One plausible explanation is the transamination of the three acids to produce glutamic acid in cancerous cells.

摘要

谷氨酸和丙氨酸占人体总氨基酸的 60%以上。谷氨酰胺是细胞的重要能量来源,也是许多氨基酸生物合成中氮的主要供体。多项研究主张谷氨酸在癌症治疗中的作用。鉴定癌细胞中的代谢特征对于基于细胞代谢状态的癌症治疗的进展至关重要。稳定的氮同位素比值(N/N,δN)对于了解癌细胞的代谢状态特别有利,因为大多数生化反应都涉及氮的转移。在我们的研究中,我们使用人结直肠癌细胞系中单个氨基酸的氮同位素自然丰度(δN 值)来研究氨基酸之间的同位素歧视。在谷氨酸、丙氨酸、天冬氨酸和脯氨酸的情况下,在癌细胞和健康细胞之间观察到了显著的影响。数据表明,在癌细胞中,谷氨酸是氮的接受体,而丙氨酸、天冬氨酸和脯氨酸是氮的供体。一个合理的解释是这三种酸在癌细胞中转氨基生成谷氨酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb2/5451381/c49d2580ea0c/41598_2017_2793_Fig1_HTML.jpg

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